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251 results for “herbicides”

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zenodo28/100

Fig. 6 in Potential herbicidal effect of synthetic chalcones on the initial growth of sesame, Sesamum indicum L., and brachiaria, Urochloa decumbens (Stapf) R. D. Webster

Fig. 6. Percentage of growth inhibition/stimulus of root parts of brachiaria seedlings [Urochloa decumbens (Stapf)R.D. Webster] grown for five days in water solutions containing the chalcones, or analogues, or Glyphosate®, in comparison to the positive control (distilled water). The chalcones are identified in the figure 2. *Indicates a significant difference in relation to the control, p<0.05.

opencc-by-4.0May 2018View details →
zenodo28/100

Fig. 3 in Potential herbicidal effect of synthetic chalcones on the initial growth of sesame, Sesamum indicum L., and brachiaria, Urochloa decumbens (Stapf) R. D. Webster

Fig. 3. Percentage of growth inhibition/stimulus of shoot parts of sesame seedlings (Sesamum indicum L.) grown for five days in water solutions containing the chalcones, or analogues, or Glyphosate®, in comparison to the positive control (distilled water). The chalcones are identified in figure 2. *Indicates a significant difference in relation to the control, p<0.05.

opencc-by-4.0May 2018View details →
dryad28/100

Data from: The experimental evolution of herbicide-resistance in Chlamydomonas reinhardtii results in a positive correlation between fitness in the presence and absence of herbicides

Pleiotropic fitness trade-offs will be key determinants of the evolutionary dynamics of selection for pesticide resistance. However, for herbicide resistance, empirical support for a fitness cost of resistance is mixed, and it is therefore also questionable what further ecological trade-offs can be assumed to apply to herbicide resistance. Here, we test the existence of trade-offs by experimentally evolving herbicide resistance in Chlamydomonas reinhardtii. Although fitness costs are detected for all herbicides, we find that, counterintuitively, the most resistant populations also have the lowest fitness costs as measured by growth rate in the ancestral environment. Furthermore, after controlling for differences in the evolutionary dynamics of resistance to different herbicides, we also detect significant positive correlations between resistance, fitness in the ancestral environment and cross-resistance to other herbicides. We attribute this to the highest levels of nontarget-site resistance being achieved by fixing mutations that more broadly affect cellular physiology, which results in both more cross-resistance and less overall antagonistic pleiotropy on maximum growth rate. Consequently, the lack of classical ecological trade-offs could present a major challenge for herbicide resistance management.

opencc-zeroDec 2011View details →
zenodo28/100

Fig. 4 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae

Fig. 4. Experimental and calculated ECD spectra of 1–4 and 8.

opennotspecifiedFeb 2023View details →
zenodo28/100

Fig. 7 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae

Fig. 7. Symptoms of 1–4 and 8 against the weed seeding growth of S. viridis.

opennotspecifiedFeb 2023View details →
zenodo28/100

Fig. 3 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae

Fig. 3. Key NOE correlations of 1–5 and 8.

opennotspecifiedFeb 2023View details →
zenodo28/100

Fig. 6 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae

Fig. 6. Effect of different specialized metabolites on seed germination of S. viridis.

opennotspecifiedFeb 2023View details →
zenodo28/100

Fig. 1 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae

Fig. 1. Chemical structures of 1–8.

opennotspecifiedFeb 2023View details →
zenodo28/100

Fig. 2. Key 1H–1H in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae

Fig. 2. Key 1H–1H COSY, and HMBC correlations of 1–5 and 8.

opennotspecifiedFeb 2023View details →
dryad28/100

Data from: Effects of biochar on fate and toxicity of herbicide fenoxaprop-ethyl in soil

Open the record for dataset details and reuse information.

publicMar 2018View details →
dryad28/100

Data from: The experimental evolution of herbicide-resistance in Chlamydomonas reinhardtii results in a positive correlation between fitness in the presence and absence of herbicides

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publicJul 2012View details →
dryad28/100

Data from: Perinatal exposure to glyphosate and a glyphosate-based herbicide affect spermatogenesis in mice

Open the record for dataset details and reuse information.

publicFeb 2019View details →
dryad28/100

Data from: Herbicides and herbivory interact to drive plant community and crop-tree establishment

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publicJun 2018View details →
dryad28/100

Data from: The geographic mosaic of herbicide resistance evolution in the common morning glory, Ipomoea purpurea: evidence for resistance hotspots and low genetic differentiation across the landscape

Open the record for dataset details and reuse information.

publicJun 2015View details →
nasa28/100

BOREAS TGB-07 Ambient Air Herbicide and Organochlorine Concentration Data

The BOREAS TGB-07 team measured the concentration and flux of several agricultural pesticides in air, rainwater, and dry deposition samples in order to determine the associated yearly deposition rates. This data set contains information on the ambient air concentration of seven herbicides [2,4-dichlorophenoxyacidic_acid (2,4-D), bromoxynil, dicamb, 2-methyl-4-chlorophenoxyacetic acid (MCPA), triallate, trifluralin, and diclop-methyl] known to appear in the atmosphere of the Canadian prairies. Also, the concentration of three herbicides (atrazine, alaclor and metolachlor), two groups of insecticides (lindane and breakdown products and dichlro-diphenyl-trichloroethane (DDT) and breakdown products), and several polychlorinated biphenyls commonly used in the central United States were measured. All of these chemicals are reported, in the literature, to be transported in the atmosphere. Many have been reported to occur in boreal and arctic food chains. The sampling was carried out from June 16 to August 13, 1993 and May 4 to July 20, 1994 at the BOREAS site in the Prince Albert National Park (Waskesiu).

restrictednotspecifiedApr 2025View details →
nasa28/100

BOREAS TGB-07 Rainwater Herbicide and Organochlorine Concentration Data

The BOREAS TGB-07 team measured the concentration and flux of several agricultural pesticides in air and rainwater samples in order to determine the associated yearly deposition rates. This data set contains information on the rainwater concentration of seven herbicides [2,4-dichlorophenoxyacidic_acid (2,4-D), bromoxynil, dicamb, 2-methyl-4-chlorophenoxyacetic acid (MCPA), triallate, trifluralin, and diclop-methyl] known to appear in the atmosphere of the Canadian prairies. Also, the concentration of three herbicides (atrazine, alaclor and metolachlor), two groups of insecticides (lindane and breakdown products and dichlro-diphenyl-trichloroethane (DDT) and breakdown products), and several polychlorinated biphenyls commonly used in the central United States were measured. All of these chemicals are reported, in the literature, to be transported in the atmosphere. Many have been reported to occur in boreal and arctic food chains. The sampling was carried out from June 16 to August 13, 1993 and May 4 to July 20, 1994 at the BOREAS site in the Prince Albert National Park (Waskesiu).

restrictednotspecifiedApr 2025View details →
nasa28/100

BOREAS TGB-07 Dry Deposition Herbicide and Organochlorine Flux Data

The BOREAS TGB-07 team measured the concentration and flux of several agricultural pesticides in air, rainwater, and dry deposition samples in order to determine the associated yearly deposition rates. This data set contains information on the dry deposition flux of seven herbicides [2,4-dichlorophenoxyacidic_acid (2,4-D), bromoxynil, dicamb, 2-methyl-4-chlorophenoxyacetic acid (MCPA), triallate, trifluralin, and diclop-methyl] known to appear in the atmosphere of the Canadian prairies. Also, the concentration of three herbicides (atrazine, alaclor and metolachlor), two groups of insecticides (lindane and breakdown products and dichlro-diphenyl-trichloroethane (DDT) and breakdown products), and several polychlorinated biphenyls commonly used in the central United States were measured. All of these chemicals are reported, in the literature, to be transported in the atmosphere. Many have been reported to occur in boreal and arctic food chains. The sampling was carried out from June 16 to August 13, 1993 and May 4 to July 20, 1994 at the BOREAS site in the Prince Albert National Park (Waskesiu).

restrictednotspecifiedApr 2025View details →
geo24/100

Non-target site herbicide resistance is conferred by two distinct mechanisms in blackgrass (Alopecurus myosuroides)

GEO Series GSE162422. Alopecurus myosuroides. 15 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJan 2021View details →
geo24/100

Transcriptome analysis indicates the involvement of herbicide-responsive and plant-pathogen interaction pathways in the development of resistance to ACCase inhibitors in Apera spica-venti

GEO Series GSE204788. Apera spica-venti. 2 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenApr 2023View details →
geo24/100

Transcript profiles of juvenile female brown trout exposed to glyphosate and Roundup herbicides.

GEO Series GSE56855. Salmo trutta. 45 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenApr 2015View details →

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